EP1192906A1 - Shunt intra-artériel et procédé d'utilisation - Google Patents

Shunt intra-artériel et procédé d'utilisation Download PDF

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Publication number
EP1192906A1
EP1192906A1 EP01120787A EP01120787A EP1192906A1 EP 1192906 A1 EP1192906 A1 EP 1192906A1 EP 01120787 A EP01120787 A EP 01120787A EP 01120787 A EP01120787 A EP 01120787A EP 1192906 A1 EP1192906 A1 EP 1192906A1
Authority
EP
European Patent Office
Prior art keywords
shunt tube
section
intra
large diameter
tube
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP01120787A
Other languages
German (de)
English (en)
Inventor
Masayoshi Okada
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nipro Corp
Original Assignee
Nipro Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nipro Corp filed Critical Nipro Corp
Publication of EP1192906A1 publication Critical patent/EP1192906A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
    • A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/11—Surgical instruments, devices or methods, e.g. tourniquets for performing anastomosis; Buttons for anastomosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
    • A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
    • A61B17/12027—Type of occlusion
    • A61B17/12036—Type of occlusion partial occlusion
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
    • A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
    • A61B17/12027—Type of occlusion
    • A61B17/1204—Type of occlusion temporary occlusion
    • A61B17/12045—Type of occlusion temporary occlusion double occlusion, e.g. during anastomosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
    • A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
    • A61B17/12099—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder
    • A61B17/12109—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder in a blood vessel
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
    • A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
    • A61B17/12131—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
    • A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
    • A61B17/12131—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device
    • A61B17/12181—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device formed by fluidized, gelatinous or cellular remodelable materials, e.g. embolic liquids, foams or extracellular matrices
    • A61B17/1219—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device formed by fluidized, gelatinous or cellular remodelable materials, e.g. embolic liquids, foams or extracellular matrices expandable in contact with liquids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/04—Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • A61F2/06—Blood vessels
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
    • A61F2/2493—Transmyocardial revascularisation [TMR] devices
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/00234—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery
    • A61B2017/00238—Type of minimally invasive operation
    • A61B2017/00243—Type of minimally invasive operation cardiac
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/11—Surgical instruments, devices or methods, e.g. tourniquets for performing anastomosis; Buttons for anastomosis
    • A61B2017/1135—End-to-side connections, e.g. T- or Y-connections
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
    • A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
    • A61B2017/12127—Double occlusion, e.g. for creating blood-free anastomosis site

Definitions

  • the invention relates to devices for use in restricting bleeding during a surgery by stopping an artery blood flow, the devices maintaining a blood flow through a lumen of a shunt tube, and more particularly, to the shunt tube effective in a coronary artery bypass surgery.
  • MIDCAB minimally invasive direct coronary artery bypass
  • Japanese Patent Laid-Open No. 127772/1998 proposes use of a catheter provided with balloons at remote ends thereof.
  • the catheter 50 is inserted into an inside of a blood vessel 54 through an incised section 56 holding an original elongate shape thereof without inflating the balloons 52 and, then, as shown in FIG. 10B, the balloons 52 are inflated until they strongly press against an inner wall of the blood vessel 54 whereupon blood which flows inside the blood vessel 54 is blocked on a part flowing along the inner wall of the blood vessel 54 and allowed to flow through the catheter 50 from a proximal side to a distal side.
  • expected is an effect that, owing to no blood flow in a neighborhood of the incised section 56, there is no bleeding therefrom and, at the same time, blood flow to the distal side is secured thereby causing no myocardial ischemia.
  • a gist of an intra-arterial shunt tube according to the present invention is in comprising a lumen having an opening on each end of the lumen, a flexible tube, and a large diameter section made of plastic and positioned on each end of the flexible tube.
  • the plastic for forming the large diameter section is a shape memory resin.
  • the plastic for forming the large diameter member is a water-swellable resin.
  • a gist of a method of using an intra-arterial shunt tube according to the present invention is in comprising a lumen having an opening on each end of the lumen, a flexible tube, and a large diameter section made of plastic and positioned on each end of the flexible tube, the method further comprising the steps of:
  • the large diameter section of the shunt tube is made of a shape memory resin or a water-swellable resin, and, after the shunt tube is set in a predetermined location straddling the incised section of the artery, a diameter of the large diameter section is enlarged.
  • the shunt tube is retracted from the incised section while being folded by pulling a string previously tied to the shunt tube in the middle.
  • FIG. 1 shows an example of an intra-arterial shunt tube according to the present invention which is a shunt tube 10 in a dumbbell-like shape comprising a flexible tube 12 provided with a large diameter section 14 positioned on each end having an opening thereof.
  • the shunt tube 10 is tied to one end of a string 16 in the middle and the other end of the string 16 is tied to a ring 18.
  • the shunt tube 10 can be used for incision surgery of, for example, an internal carotid artery and an external carotid artery, it is effective in preventing occurrence of cerebral ischemia which is apt to lead a grave consequence, when it is particularly used for a coronary artery bypass surgery.
  • the coronary artery 20 is attached to an outside of the heart 22 to supply blood to heart muscle.
  • blood supply to the heart muscle becomes deficient to bring about myocardial ischemia.
  • the shunt tube 10 is inserted to a proximal side 28 of a location in which a first diagonal branch 23 is branched from a principal trunk 21 of the coronary artery 20.
  • the shunt tube 10 is inserted through the incised section 24 of the coronary artery 20 and, as shown in FIG. 3, straddles the incised section 24 and, then, is set in a location in which the large diameter section 14 is positioned on each side of the incised section 24.
  • the ring 18 tied to the string 16 is placed outside the incised section 24. It is convenient to perform work as described above for inserting or registering the shunt tube 10 by using a forceps or other appropriate instruments.
  • the shunt tube 10 is retracted from the incised section 24 before anastomosis is completed. As shown in FIG. 4, when the ring 18 is pulled, the shunt tube 10 is folded in half guided by the string 16 and is retracted from the incised section 24 and, finally, the large diameter section 14 thereof is retracted. Then, a section on which anastomosis is yet to be performed is quickly sutured to complete the anastomosis.
  • the shunt tube 10 is arranged such that the length and diameter thereof correspond to an artery to be incised.
  • an entire length of 40 mm, a length on each large diameter section 14 of 4 mm, a diameter of the tube 12 of 3 mm and a diameter of each large diameter section 14 of about 4 mm are adopted.
  • a length of 70 mm to 100 mm and a diameter of the large diameter section of about 6 mm are adopted. Accordingly, as long as the shunt tube 10 provided with the large diameter section 14 having a diameter of about 1.0 mm to about 6 mm is prepared, almost all arteries may be treated.
  • Retraction of the shunt tube 10 from the incised section 24 can be executed by nipping it in the middle by forceps or other instruments; however, as described above, once the string 16 tied to the ring 18 has previously been tied to the shunt tube 10 in the middle, the shunt tube 10 can be retracted by pulling the ring 18 easily and very conveniently. Further, once a piece of a board, instead of the ring 18, on which a size and other information of the shunt tube 10 are manifested has been tied to the string 16, features of the shunt tube 10 can assuredly be confirmed before it is used so that a trouble such as incompatibility with an artery to be treated can be avoided, which is effective in securing safety.
  • the shunt tube 10 is constituted simply by the flexible tube 12 and the large diameter section 14 positioned on each end thereof. Since the tube 12 is flexible, the tube 12 positioned directly under the incised section 24 can easily be retracted while being nipped and folded in half.
  • Materials for use in the tube 12 are not particularly limited, but those to be used in ordinary catheters such as polyvinyl chloride, polyurethane, silicone, polyethylene and polypropylene are preferably used.
  • the material for use in the large diameter section 14 is not particularly limited, either. As shown in FIG. 5, the section 14 may be molded integrally with the tube 12 by using the same material as that of the tube 12. As shown in FIGS. 6 and 7, the material for use in the large diameter section 14 may of course be different from that of the tube 12; in the shunt tube 10 as shown in FIG. 6, the large diameter section 14 is formed by covering each end of the tube 12 with an annular member 32; in the shunt tube 10 as shown in FIG. 7, the large diameter section 14 is formed by connecting the annular member 32 having a large diameter such that each end of the tube 12 is extended.
  • the same plastic material as that of the tube 12 inclusive of a porous material thereof a cellulose type resin, a water-swellable type resin, a shape memory resin and other appropriate resins are preferably used and, among others, the water-swellable type resin and shape memory resin are particularly useful.
  • a fatty deposit such as cholesterol is attached to an inner wall of an artery proximate to the incised section 24 into which the shunt tube 10 is inserted whereupon the deposit is liable to be pushed inwardly in the artery at a location of the large diameter section 14 when the shunt tube 10 is inserted.
  • the artery may be narrowed or a plaque may be formed. This occurrence is not favorable since use of the shunt tube 10 brings about an adverse effect.
  • the large diameter section 14 is small in diameter so as to prevent the deposit from being pushed inwardly and, then, once the shunt tube 10 has been set at a predetermined location, the diameter of the large diameter section 14 is enlarged so as to stop blood flow.
  • the large diameter section 14 made of a water-swellable resin intends to make use of a property that it gains volume as swells with water. Namely, as illustrated in FIGS. 8A and 8B, when inserted in the artery through the incised section 24, the large diameter section 14 is in a dry, fine state and, then, when set in a predetermined local ion straddling the incised section 24, the large diameter section 14 contacts blood, swells and becomes thick.
  • the large diameter section 14 does not scrape the fatty deposit build up on the inner wall of the artery when inserted and, moreover, it becomes possible to stop blood flow into the incised section 24 in an assured manner.
  • the water-swellable resin to be used in the present invention has following requirements as characteristics to be imparted at the time of swelling with water:
  • a resin which swells into as much as about 1.1 time to about 3.0 times the weight of the resin itself at a temperature proximate to body temperature in 15 minutes.
  • an acrylate type starch-grafted product a partially saponified polyvinyl alcohol, a polyacrylic salt type polymer, an acrylic-vinyl alcohol type polymer, polyethylene oxide and cellulose type polymer are exemplified.
  • Swelling characteristics can be controlled by optimally selecting a polymerization degree of a polymer constituting each plastic, a copolymerization or blending ratio the re of with another polymer, and a cross-linking degree thereof.
  • the large diameter section 14 is made of a shape memory resin, it is intended that deformation characteristics, instead of the volume increase thereof, that an original shape which has previously been memorized can be recovered when a temperature of the section 14 exceeds transition temperature thereof is utilized. Namely, as illustrated in FIG. 9, when inserted in the incised section 24, the large diameter section 14 is previously deformed in a fine state and cooled while being held in the state; then, the section 14 is set in a predetermined location in the artery. It is arranged that, when the temperature of the section 14 comes near to body temperature, the large diameter section 14 recovers its original shape of large diameter.
  • the large diameter section 14 is fine at the time of insertion and becomes thick at the time of being positioned at the predetermined location in the artery so that it assuredly stops blood flow into the incised section 24.
  • shape memory resin those having a transition temperature close to body temperature, that is, from 35°C to 37°C are preferable; polyacrylamide and polyacrylic acid and other appropriate compounds can be used.
  • blood flow into an incised section can be restricted by a large diameter section positioned on each end of the shunt tube and blood can be flowed from a proximal side to a distal side through a lumen inside the shunt tube so that a coronary artery bypass surgery can be performed in a leisurely, safe, assured manner without causing myocardial ischemia.
  • the large diameter section is made of resin hard to be deformed, restriction of blood flow into the incised section can assuredly be maintained for a long period of time whereupon troubles such as a large quantity of bleeding from the incised section can be prevented. Still further, since a flexible tube is used, the tube can be folded in half and retracted from the artery in an easy manner.
  • the large diameter section is made of a water-swellable resin, it can take a fine configuration in a dry state at the time of insertion from the incised section and, once it is set at a predetermined location in the artery, it can be swelled/expanded by contacting blood whereupon the shunt tube which has greatly been improved in insertion property and substantially been enhanced in safety can be obtained.
  • the large diameter section is made of a shape memory resin
  • the method of using the intra-arterial shunt tube according to the present invention can be performed by so simple a work as to handle the shunt tube only by, for example, forceps without necessitating preparation of, for example, a compressor.
  • the shunt tube can be retracted from the artery while the flexible tube is nipped in the middle and folded in half in a simple manner.
  • the tube can be retracted by pulling the string in a simpler manner.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • General Health & Medical Sciences (AREA)
  • Vascular Medicine (AREA)
  • Molecular Biology (AREA)
  • Medical Informatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Reproductive Health (AREA)
  • Cardiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Pulmonology (AREA)
  • Surgical Instruments (AREA)
  • Prostheses (AREA)
  • Media Introduction/Drainage Providing Device (AREA)
EP01120787A 2000-09-28 2001-09-10 Shunt intra-artériel et procédé d'utilisation Withdrawn EP1192906A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2000296320 2000-09-28
JP2000296320A JP2002102260A (ja) 2000-09-28 2000-09-28 動脈内のシャントチューブ及びその使用方法

Publications (1)

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EP1192906A1 true EP1192906A1 (fr) 2002-04-03

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US (1) US20020038100A1 (fr)
EP (1) EP1192906A1 (fr)
JP (1) JP2002102260A (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1584304A1 (fr) * 2004-04-08 2005-10-12 KRAUTH medical KG (GmbH & Co.) Un conduit à introduire dans un vaisseau sanguin
WO2014067021A3 (fr) * 2012-10-29 2014-06-26 Endoheart Ag Dispositif de fermeture
US8906081B2 (en) 2007-09-13 2014-12-09 W. L. Gore & Associates, Inc. Stented vascular graft
US9375215B2 (en) 2006-01-20 2016-06-28 W. L. Gore & Associates, Inc. Device for rapid repair of body conduits
EP4190284A4 (fr) * 2020-07-28 2024-07-24 Sparkle Medical Equipment Shanghai Co Ltd Dilatateur-support d'anastomose de lumière

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US6605053B1 (en) 1999-09-10 2003-08-12 Percardia, Inc. Conduit designs and related methods for optimal flow control
JP3849140B2 (ja) 2002-10-30 2006-11-22 ニプロ株式会社 血管把持具
US9498366B2 (en) * 2003-07-28 2016-11-22 Baronova, Inc. Devices and methods for pyloric anchoring
US9700450B2 (en) 2003-07-28 2017-07-11 Baronova, Inc. Devices and methods for gastrointestinal stimulation
US20090259236A2 (en) * 2003-07-28 2009-10-15 Baronova, Inc. Gastric retaining devices and methods
US8821521B2 (en) 2003-07-28 2014-09-02 Baronova, Inc. Gastro-intestinal device and method for treating addiction
US8048169B2 (en) * 2003-07-28 2011-11-01 Baronova, Inc. Pyloric valve obstructing devices and methods
US20070203452A1 (en) * 2003-10-07 2007-08-30 Mehta Bharat A Platform Catheter
US20070260262A1 (en) * 2004-08-30 2007-11-08 Sosuke Kimura Supporting Device for Coronary Artery Bypass Surgery
AU2008296110B2 (en) * 2007-09-07 2013-03-14 Baronova, Inc. Device for intermittently obstructing a gastric opening and method of use
BR112015023344B1 (pt) 2013-03-15 2022-05-31 Baronova, Inc Dispositivo para intermitentemente obstruir uma abertura gástrica; e método de reconfiguração instalação de um dispositivo de oclusão
CN113041482B (zh) * 2021-03-05 2022-08-12 深圳市赛诺思医疗科技有限公司 动脉分流栓

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JPS6427772A (en) 1987-07-22 1989-01-30 Matsushita Electric Ind Co Ltd Substrate heating device
US4957508A (en) * 1986-10-31 1990-09-18 Ube Industries, Ltd. Medical tubes
DE4412262A1 (de) * 1994-04-09 1995-10-12 Herbert Prof Dr Med Imig Intraluminaler Arbeitsshunt für Endovascular-Technik in der Gefäßchirurgie
EP0791332A1 (fr) * 1996-02-20 1997-08-27 Cardiothoracic Systems, Inc. Un dispositif de perfusion pour maintenir le flux de sang dans un vesseau pendant und procédé d'anastomose
JPH11335A (ja) * 1997-06-10 1999-01-06 Jms Co Ltd 血管吻合補助具
US5868764A (en) * 1996-12-12 1999-02-09 Cornell Research Foundation, Inc. Perfusion and occlusion device and method
WO1999023955A1 (fr) * 1997-11-12 1999-05-20 Robert Lazzara Dispositif de pontage vasculaire
US5964744A (en) * 1993-01-04 1999-10-12 Menlo Care, Inc. Polymeric medical device systems having shape memory

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4957508A (en) * 1986-10-31 1990-09-18 Ube Industries, Ltd. Medical tubes
JPS6427772A (en) 1987-07-22 1989-01-30 Matsushita Electric Ind Co Ltd Substrate heating device
US5964744A (en) * 1993-01-04 1999-10-12 Menlo Care, Inc. Polymeric medical device systems having shape memory
DE4412262A1 (de) * 1994-04-09 1995-10-12 Herbert Prof Dr Med Imig Intraluminaler Arbeitsshunt für Endovascular-Technik in der Gefäßchirurgie
EP0791332A1 (fr) * 1996-02-20 1997-08-27 Cardiothoracic Systems, Inc. Un dispositif de perfusion pour maintenir le flux de sang dans un vesseau pendant und procédé d'anastomose
US5868764A (en) * 1996-12-12 1999-02-09 Cornell Research Foundation, Inc. Perfusion and occlusion device and method
JPH11335A (ja) * 1997-06-10 1999-01-06 Jms Co Ltd 血管吻合補助具
WO1999023955A1 (fr) * 1997-11-12 1999-05-20 Robert Lazzara Dispositif de pontage vasculaire

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Title
PATENT ABSTRACTS OF JAPAN vol. 1999, no. 04 30 April 1999 (1999-04-30) *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1584304A1 (fr) * 2004-04-08 2005-10-12 KRAUTH medical KG (GmbH & Co.) Un conduit à introduire dans un vaisseau sanguin
US9375215B2 (en) 2006-01-20 2016-06-28 W. L. Gore & Associates, Inc. Device for rapid repair of body conduits
US9381018B2 (en) 2006-01-20 2016-07-05 W. L. Gore & Associates, Inc. Device for rapid repair of body conduits
US10357352B2 (en) 2006-01-20 2019-07-23 W. L. Gore & Associates, Inc. Device for rapid repair of body conduits
US8906081B2 (en) 2007-09-13 2014-12-09 W. L. Gore & Associates, Inc. Stented vascular graft
US9107744B2 (en) 2007-09-13 2015-08-18 W. L. Gore & Associates, Inc. Stented vascular graft
US9295542B2 (en) 2007-09-13 2016-03-29 W. L. Gore & Associates, Inc. Stented vascular graft
US10080643B2 (en) 2007-09-13 2018-09-25 W. L. Gore Associates, Inc. Stented vascular graft
US11547548B2 (en) 2007-09-13 2023-01-10 W. L. Gore & Associates, Inc. Stented vascular graft
WO2014067021A3 (fr) * 2012-10-29 2014-06-26 Endoheart Ag Dispositif de fermeture
EP4190284A4 (fr) * 2020-07-28 2024-07-24 Sparkle Medical Equipment Shanghai Co Ltd Dilatateur-support d'anastomose de lumière

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